$29.23
Clear TestWeight: 0.25kg
SKU: 6282Clear DOA COMBO-6 Test Surestep Drug Screen Panel is a test designed to determine the quantities of opioid and narcotic substances in human urine specifics. The test is intended to simultaneously study Camfetamine, methadone, cocaine, methamphetamine, opiates (heroin, morphine, codeine), marijuana. Each cassette based on a specific immuno-chemical reaction between antibodies and antigens to analyze a particular specific component of human urine specimen. The plate reports the competition for binding the antibodies. When a medicine is present in urine specimen, it comprises the drug compounds for the limited amount of antibody-colored compound. When the amount of medicament is equal to or more than the limit, it will prevent the binding of the opiate compound with the antibodies. Therefore, a positive urinary specimen will not show a colored strip in the test area, marking a positive result while the presence of a colored strip indicates or means a negative result. The control line is present in the test window to serve to control the procedure. This colored strip should always appear on the control line area if the test device is stored in good condition and the test is done correctly.
COMPOSITION OF THE CLEAR DOA COMBO-6 Combined drug and opiate test, 6 parameters, cassette. In the package you will find: Box with 6pc test strips on 1 panel. Instructions for use. Required materials that are not produced: A urine collection container Timer or clock
Clear DOA COMBO-6 Combined Drug and Opinion Test, 6 parameters, cassette. Collection of specifics and preparation: Fresh urine does not require any special processing or pre-treatment. If the quantitative analysis is not presented instantly urinary sponsion can be frozen or placed in a refrigerator at a temperature of 2 to 8 degrees for up to 7 days. Before testing, samples should be left to reach room temperature. Urine specimens showing increased sludge or turbidity should be centrifuged or allowed to settle before testing. Quality control: The control bar is an internal reagent and control of the procedure. It will appear if the test is performed correctly and the reagents are reactivated. Control standards can be used to validate the performance of the reagents and to establish the reliability of the test. Procedure: 1. Warm all materials and specimens to room temperature. 2. Remove the test card and the sealed plastic cap to open the foil box. 3. Place the end of the sampling pad in urine specimen you are careful to keep the trick in the urine so that you do not touch the plastic card. 4. Keep the card in the urine 10 seconds, remove it from the urine and put the cap again. 5. Read the result after 5 minutes. Never interpret result in 10 minutes! Interpreting the results: Negative: Two colored stripes appear. The appearance of two stained strips one in the test area line and one in the control line area indicates negative results. The negative result does not show the absence of opiates in the specimen. It only indicates that the drug level in the specimen is less, lower than the permissible level. Positive: One stained band appears in the control line area. No colored tape is detected in the test line zone. This is an indication that the level of drug in urine specimen is over the permissible limit. Invalid: If there is no colored strip in the control line area - the result of the test is invalid. Test the sample with a new test device. Note: A very slightly colored strip in the test line area indicates that the amount of amphetamine in the sample is close to the level of a permissible limit. These specimen and other positive samples should be confirmed by using an alternative method such as GC / MS
Used only for diagnosis in vitro or for legal, judicial expertise Use the product after the expiry date; Work with all specimens as if they are potential infectiousness open the metal, foil box until it is ready for the test; Use a new urine specimen for each sample to prevent cross contamination; The test should be stored at a temperature of 2 to 30 degrees and will be effective to the shelf life specified;